Inhibition gates supralinear Ca2+ signaling in Purkinje cell dendrites during practiced movements

Motor learning involves neural circuit modifications in the cerebellar cortex, likely through re-weighting of parallel fiber inputs onto Purkinje cells (PCs). Climbing fibers instruct these synaptic modifications when they excite PCs in conjunction with parallel fiber activity, a pairing that enhances climbing fiber-evoked Ca2+ signaling in PC dendrites. In vivo, climbing fibers spike continuously, including during movements when parallel fibers are simultaneously conveying sensorimotor information to PCs. Whether parallel fiber activity enhances climbing fiber Ca2+ signaling during motor behaviors is unknown. In mice, we found that inhibitory molecular layer interneurons (MLIs), activated by parallel fibers during practiced movements, suppressed parallel fiber enhancement of climbing fiber Ca2+ signaling in PCs. Similar results were obtained in acute slices for brief parallel fiber stimuli. Interestingly, more prolonged parallel fiber excitation revealed latent supralinear Ca2+ signaling. Therefore, the balance of parallel fiber and MLI input onto PCs regulates concomitant climbing fiber Ca2+ signaling.

[1]  Masao Ito,et al.  Climbing fibre induced depression of both mossy fibre responsiveness and glutamate sensitivity of cerebellar Purkinje cells , 1982, The Journal of physiology.

[2]  Arvind Kumar,et al.  Short-Term Plasticity Combines with Excitation–Inhibition Balance to Expand Cerebellar Purkinje Cell Dynamic Range , 2018, The Journal of Neuroscience.

[3]  Masao Ito,et al.  Long-lasting depression of parallel fiber-Purkinje cell transmission induced by conjunctive stimulation of parallel fibers and climbing fibers in the cerebellar cortex , 1982, Neuroscience Letters.

[4]  C. Hansel,et al.  Bidirectional Parallel Fiber Plasticity in the Cerebellum under Climbing Fiber Control , 2004, Neuron.

[5]  George J Augustine,et al.  Serial processing of kinematic signals by cerebellar circuitry during voluntary whisking , 2017, Nature Communications.

[6]  M. Häusser,et al.  Integration of quanta in cerebellar granule cells during sensory processing , 2004, Nature.

[7]  Anirvan Ghosh,et al.  Chemogenetic Synaptic Silencing of Neural Circuits Localizes a Hypothalamus→Midbrain Pathway for Feeding Behavior , 2014, Neuron.

[8]  M. Häusser,et al.  Encoding of Oscillations by Axonal Bursts in Inferior Olive Neurons , 2009, Neuron.

[9]  Thomas M. Morse,et al.  Compartmentalization of GABAergic Inhibition by Dendritic Spines , 2013, Science.

[10]  S. Wang,et al.  Reliable Coding Emerges from Coactivation of Climbing Fibers in Microbands of Cerebellar Purkinje Neurons , 2009, The Journal of Neuroscience.

[11]  Rafael Yuste,et al.  Fast nonnegative deconvolution for spike train inference from population calcium imaging. , 2009, Journal of neurophysiology.

[12]  Giorgio Grasselli,et al.  Calcium threshold shift enables frequency-independent control of plasticity by an instructive signal , 2016, Proceedings of the National Academy of Sciences.

[13]  The Roles , 2020, Web and Digital for Graphic Designers.

[14]  Stefan R. Pulver,et al.  Ultra-sensitive fluorescent proteins for imaging neuronal activity , 2013, Nature.

[15]  G. Augustine,et al.  Calcium as a Trigger for Cerebellar Long-Term Synaptic Depression , 2012, The Cerebellum.

[16]  Arnd Roth,et al.  Structured Connectivity in Cerebellar Inhibitory Networks , 2014, Neuron.

[17]  J. Christie,et al.  Chronic imaging of movement-related Purkinje cell calcium activity in awake behaving mice. , 2016, Journal of neurophysiology.

[18]  Claire E McKellar,et al.  Rational design of a high-affinity, fast, red calcium indicator R-CaMP2 , 2014, Nature Methods.

[19]  Michael A. Gaffield,et al.  Movement Rate Is Encoded and Influenced by Widespread, Coherent Activity of Cerebellar Molecular Layer Interneurons , 2017, The Journal of Neuroscience.

[20]  Ian Duguid,et al.  Dendritic excitation–inhibition balance shapes cerebellar output during motor behaviour , 2016, Nature Communications.

[21]  H. Taniguchi,et al.  Using c-kit to genetically target cerebellar molecular layer interneurons in adult mice , 2017, PloS one.

[22]  Yan Yang,et al.  Duration of complex-spikes grades Purkinje cell plasticity and cerebellar motor learning , 2014, Nature.

[23]  Javier F. Medina,et al.  Sensory-Driven Enhancement of Calcium Signals in Individual Purkinje Cell Dendrites of Awake Mice , 2014, Cell reports.

[24]  Ben Deverett,et al.  Cerebellar granule cells acquire a widespread predictive feedback signal during motor learning , 2017, Nature Neuroscience.

[25]  M. Kano,et al.  Long-term depression of parallel fibre synapses following stimulation of climbing fibres , 1985, Brain Research.

[26]  C. Hansel,et al.  The Making of a Complex Spike: Ionic Composition and Plasticity , 2002, Annals of the New York Academy of Sciences.

[27]  D. Harriman CEREBELLAR CORTEX, CYTOLOGY AND ORGANIZATION , 1974 .

[28]  B. Roth,et al.  Evolving the lock to fit the key to create a family of G protein-coupled receptors potently activated by an inert ligand , 2007, Proceedings of the National Academy of Sciences.

[29]  Conor Liston,et al.  Projections from neocortex mediate top-down control of memory retrieval , 2015, Nature.

[30]  Stephen G. Lisberger,et al.  Links from complex spikes to local plasticity and motor learning in the cerebellum of awake-behaving monkeys , 2008, Nature Neuroscience.

[31]  W. T. Thach,et al.  Purkinje cell activity during motor learning , 1977, Brain Research.

[32]  H. Hirai,et al.  Minimal Purkinje Cell-Specific PCP2/L7 Promoter Virally Available for Rodents and Non-human Primates , 2017, Molecular therapy. Methods & clinical development.

[33]  Jennifer L. Raymond,et al.  Timing Rules for Synaptic Plasticity Matched to Behavioral Function , 2018, Neuron.

[34]  D. Marr A theory of cerebellar cortex , 1969, The Journal of physiology.

[35]  W. Crill Unitary multiple-spiked responses in cat inferior olive nucleus. , 1970, Journal of neurophysiology.

[36]  J. Simpson,et al.  Visual climbing fiber input to rabbit vestibulo-cerebellum: a source of direction-specific information. , 1974, Brain research.

[37]  S. Wang,et al.  Coincidence detection in single dendritic spines mediated by calcium release , 2000, Nature Neuroscience.

[38]  M. Mauk,et al.  Inhibition of climbing fibres is a signal for the extinction of conditioned eyelid responses , 2002, Nature.

[39]  Rhea R. Kimpo,et al.  A saturation hypothesis to explain both enhanced and impaired learning with enhanced plasticity , 2017, eLife.

[40]  T. Hoogland,et al.  Behavioral Correlates of Complex Spike Synchrony in Cerebellar Microzones , 2014, The Journal of Neuroscience.

[41]  J. Nadal,et al.  Optimal Information Storage and the Distribution of Synaptic Weights Perceptron versus Purkinje Cell , 2004, Neuron.

[42]  Wade G. Regehr,et al.  Associative Short-Term Synaptic Plasticity Mediated by Endocannabinoids , 2005, Neuron.

[43]  Ruben Portugues,et al.  Sensorimotor Representations in Cerebellar Granule Cells in Larval Zebrafish Are Dense, Spatially Organized, and Non-temporally Patterned , 2017, Current Biology.

[44]  W. N. Ross,et al.  IPSPs strongly inhibit climbing fiber-activated [Ca2+]i increases in the dendrites of cerebellar Purkinje neurons , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[45]  Benjamin Mathieu,et al.  Activity-Dependent Gating of Calcium Spikes by A-type K+ Channels Controls Climbing Fiber Signaling in Purkinje Cell Dendrites , 2014, Neuron.

[46]  Rhea R. Kimpo,et al.  Gating of neural error signals during motor learning , 2014, eLife.

[47]  Henrik Jörntell,et al.  Cerebellar molecular layer interneurons – computational properties and roles in learning , 2010, Trends in Neurosciences.

[48]  Michael Häusser,et al.  Feed‐forward inhibition shapes the spike output of cerebellar Purkinje cells , 2005, The Journal of physiology.

[49]  Mark J. Schnitzer,et al.  Automated Analysis of Cellular Signals from Large-Scale Calcium Imaging Data , 2009, Neuron.

[50]  J. Eccles,et al.  The excitatory synaptic action of climbing fibres on the Purkinje cells of the cerebellum , 1966, The Journal of physiology.

[51]  M. Kawato,et al.  Ca2+ Requirements for Cerebellar Long-Term Synaptic Depression: Role for a Postsynaptic Leaky Integrator , 2007, Neuron.

[52]  D. Linden,et al.  Long-Term Depression of the Cerebellar Climbing Fiber–Purkinje Neuron Synapse , 2000, Neuron.

[53]  T. Otis,et al.  Effects of Climbing Fiber Driven Inhibition on Purkinje Neuron Spiking , 2012, The Journal of Neuroscience.

[54]  D. Tank,et al.  Widespread State-Dependent Shifts in Cerebellar Activity in Locomoting Mice , 2012, PloS one.

[55]  Kamran Khodakhah,et al.  The Role of Interneurons in Shaping Purkinje Cell Responses in the Cerebellar Cortex , 2011, The Journal of Neuroscience.

[56]  J. Weber,et al.  The role of calcium in synaptic plasticity and motor learning in the cerebellar cortex , 2012, Neuroscience & Biobehavioral Reviews.

[57]  George J Augustine,et al.  Precise Control of Movement Kinematics by Optogenetic Inhibition of Purkinje Cell Activity , 2014, The Journal of Neuroscience.

[58]  M. Häusser,et al.  Tonic Synaptic Inhibition Modulates Neuronal Output Pattern and Spatiotemporal Synaptic Integration , 1997, Neuron.

[59]  D. Todman Synapse , 2009, European Neurology.

[60]  Andreas Lüthi,et al.  Disinhibition, a Circuit Mechanism for Associative Learning and Memory , 2015, Neuron.

[61]  George J Augustine,et al.  Optogenetic mapping of cerebellar inhibitory circuitry reveals spatially biased coordination of interneurons via electrical synapses. , 2014, Cell reports.

[62]  H. Jörntell,et al.  Parallel fibre receptive fields of Purkinje cells and interneurons are climbing fibre‐specific , 2001, The European journal of neuroscience.

[63]  Farzaneh Najafi,et al.  Coding of stimulus strength via analog calcium signals in Purkinje cell dendrites of awake mice , 2014, eLife.

[64]  Javier F. Medina,et al.  Beyond “all-or-nothing” climbing fibers: graded representation of teaching signals in Purkinje cells , 2013, Front. Neural Circuits.

[65]  Mitsuo Kawato,et al.  The Roles of the Olivocerebellar Pathway in Motor Learning and Motor Control. A Consensus Paper , 2017, The Cerebellum.

[66]  William Wisden,et al.  Synaptic inhibition of Purkinje cells mediates consolidation of vestibulo-cerebellar motor learning , 2009, Nature Neuroscience.

[67]  O. Paulsen,et al.  A model of hippocampal memory encoding and retrieval: GABAergic control of synaptic plasticity , 1998, Trends in Neurosciences.

[68]  M. Häusser,et al.  Reading out a spatiotemporal population code by imaging neighbouring parallel fibre axons in vivo , 2015, Nature Communications.

[69]  A. Konnerth,et al.  Synaptic excitation produces a long-lasting rebound potentiation of inhibitory synaptic signals in cerebellar Purkinje cells , 1992, Nature.

[70]  Michael Häusser,et al.  Multimodal sensory integration in single cerebellar granule cells in vivo , 2015, eLife.

[71]  J. Spudich,et al.  Natural light-gated anion channels: A family of microbial rhodopsins for advanced optogenetics , 2015, Science.

[72]  Aapo Hyvärinen,et al.  Fast and robust fixed-point algorithms for independent component analysis , 1999, IEEE Trans. Neural Networks.

[73]  R. Keep,et al.  Brain fluid calcium concentration and response to acute hypercalcaemia during development in the rat. , 1988, The Journal of physiology.

[74]  A. Marty,et al.  Concerted Interneuron Activity in the Cerebellar Molecular Layer During Rhythmic Oromotor Behaviors , 2017, The Journal of Neuroscience.

[75]  Michael Häusser,et al.  Dendritic Calcium Signaling Triggered by Spontaneous and Sensory-Evoked Climbing Fiber Input to Cerebellar Purkinje Cells In Vivo , 2011, The Journal of Neuroscience.

[76]  J. Albus A Theory of Cerebellar Function , 1971 .